Source: ALL
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C0795687
Disease: Cerebral arterial thrombosis
Cerebral arterial thrombosis 		14 9 13 0.81 7 0.78
CUI: C0151945
Disease: Thrombosis of cerebral veins
Thrombosis of cerebral veins 		35 11 13 0.35 7 0.64
CUI: C3805092
Disease: Methylenetetrahydrofolate reductase gene mutation
Methylenetetrahydrofolate reductase gene mutation 		11 3 6 0.30 2 0.25
CUI: C0238457
Disease: Thrombosis of renal vein
Thrombosis of renal vein 		4 0 4 0.27 0 0
CUI: C0242666
Disease: Protein S Deficiency
Protein S Deficiency 		19 14 7 0.26 3 0.17
CUI: C1273976
Disease: First myocardial infarction
First myocardial infarction 		17 0 6 0.23 0 0
CUI: C2584620
Disease: Thrombophilia, hereditary
Thrombophilia, hereditary 		17 9 6 0.23 3 0.23
CUI: C0007688
Disease: Central Retinal Artery Occlusion
Central Retinal Artery Occlusion 		7 0 4 0.22 0 0
CUI: C2585317
Disease: Acquired thrombophilia
Acquired thrombophilia 		8 2 4 0.21 2 0.29
CUI: C0034341
Disease: Pyruvate Carboxylase Deficiency Disease
Pyruvate Carboxylase Deficiency Disease 		14 0 5 0.21 0 0
CUI: C0013922
Disease: Embolism
Embolism 		3 0 3 0.20 0 0
CUI: C0035302
Disease: Retinal Artery Occlusion
Retinal Artery Occlusion 		9 1 4 0.20 1 0.14
CUI: C0267412
Disease: Mesenteric Venous Thrombosis
Mesenteric Venous Thrombosis 		3 0 3 0.20 0 0
CUI: C0398621
Disease: Hypoplasminogenemia
Hypoplasminogenemia 		9 3 4 0.20 2 0.25
CUI: C0752144
Disease: Brain Thrombosis
Brain Thrombosis 		3 0 3 0.20 0 0
CUI: C0936263
Disease: Cerebral Thrombus
Cerebral Thrombus 		3 0 3 0.20 0 0
CUI: C3160844
Disease: PAI-1 polymorphism
PAI-1 polymorphism 		10 0 4 0.19 0 0
CUI: C1260403
Disease: prothrombin gene mutation
prothrombin gene mutation 		23 5 6 0.19 3 0.33
CUI: C0338573
Disease: Cerebral venous sinus thrombosis
Cerebral venous sinus thrombosis 		17 1 5 0.19 1 0.14
CUI: C0238096
Disease: Embolism, Paradoxical
Embolism, Paradoxical 		5 0 3 0.18 0 0
CUI: C0852077
Disease: Blood Coagulation Disorders, Inherited
Blood Coagulation Disorders, Inherited 		5 0 3 0.18 0 0
CUI: C0936261
Disease: Brain Thrombus
Brain Thrombus 		5 0 3 0.18 0 0
CUI: C1510431
Disease: Superficial Thrombophlebitis
Superficial Thrombophlebitis 		5 0 3 0.18 0 0
CUI: C3550150
Disease: Recurrent thrombophlebitis
Recurrent thrombophlebitis 		5 0 3 0.18 0 0
CUI: C0268615
Disease: 5,10-Methylenetetrahydrofolate reductase deficiency
5,10-Methylenetetrahydrofolate reductase deficiency 		6 6 3 0.17 1 8.3E-02